USP44 Promoter Methylation in Plasma Cell-Free DNA in Prostate Cancer.
Dora LondraSophia MastorakiEvangelos BournakisMartha ZavridouAnastasios ThanosTheodoros RampiasEvi S LianidouPublished in: Cancers (2021)
Liquid biopsy provides real-time monitoring of tumor evolution and response to therapy through analysis of circulating tumor cells (CTCs) and plasma-circulating tumor DNA (ctDNA). USP44 is a critical gene which plays an important role in cell proliferation; however, its accurate role in other cellular networks is under research. USP44 promoter methylation has been so far reported in colorectal neoplasia and metastatic breast cancer. In this study, we examined for the first time USP44 promoter methylation in plasma cell-free DNA (cfDNA) of patients with prostate cancer (early stage n = 32, metastatic n = 39) and 10 healthy donors (HD). USP44 promoter methylation was detected in plasma cell-free DNA by a newly developed highly specific and sensitive real-time MSP method. Our findings indicate that USP44 promoter is methylated in plasma cell-free DNA of metastatic prostate cancer patients and that detection of USP44 promoter methylation is significantly associated with overall survival (OS) (p = 0.008). We report for the first time that detection of USP44 promoter methylation in plasma cell free DNA provides significant prognostic information in metastatic prostate cancer.
Keyphrases
- dna methylation
- prostate cancer
- circulating tumor
- circulating tumor cells
- genome wide
- gene expression
- transcription factor
- radical prostatectomy
- early stage
- small cell lung cancer
- squamous cell carcinoma
- cell proliferation
- metastatic breast cancer
- copy number
- cell free
- healthcare
- stem cells
- radiation therapy
- cell cycle
- mesenchymal stem cells
- single molecule
- rectal cancer
- ultrasound guided
- sentinel lymph node
- health information
- free survival
- kidney transplantation
- replacement therapy